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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267448Generated: October 26, 2026

Potassium Carbonate → 1-(2-(5-Bromo-4-(5-chlorothiophen-2-yl)pyrimidin-2-ylamino)ethyl)imidazolidin-2-one

https://huagongshe.com/reaction/2267448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN-(2-Aminoethyl)ethyleneureaHCID 80480—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Bromo-2-chloro-4-(5-chlorothiophen-2-yl)pyrimidineHCID 57428833—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product1-(2-(5-Bromo-4-(5-chlorothiophen-2-yl)pyrimidin-2-ylamino)ethyl)imidazolidin-2-oneHCID 60204620—

Reaction Conditions

Temperature150 °C

Reaction Steps

5-Bromo-2-chloro-4-(5-chlorothiophen-2-yl)pyrimidine (0.4 g, 1.3 mmol), N-methyl pyrrolidone (3 mL), potassium carbonate (0.358 g, 2.6 mmol) and 1-(2-aminoethyl)-imidazolidin-2-one (0.2 g, 1.54 mmol) were all placed in a microwave tube. The reaction was heated to 150° C. for 20 min in a Personal Chemistry microwave. A saturated solution of sodium bicarbonate was added to the reaction mixture, which was extracted three times with dichloromethane. The organic layer was dried with sodium sulfate and purified by flash chromatography on silica gel using gradient of 0 to 10% methanol in dichloromethane to obtain a white solid. Yield=0.41 g. MS (M+H)+ 402/404.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858785B2
Source datasetuspto-grants-2010_12
ORD IDord-0f717531a48746a4a235f3e34b342912
Source noteuspto-grants-2010_12